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Butenafine hydrochloride

SIGMA/B5188 - ≥98% (HPLC)

Synonym: Butenafine hydrochloride; Mentax; N-(p-tert-butylbenzyl)-N-methyl-1-naphthalenemethylamine hydrochloride; N-[[4-(1,1-Dimethylethyl)phenyl]methyl]-N-methyl-1-naphthalenemethanamine hydrochloride

CAS Number: 101827-46-7
Empirical Formula (Hill Notation): C23H27N · HCl
Molecular Weight: 353.93
MDL Number: MFCD00917064
Linear Formula: C23H27N · HCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-B5188-10MG 10 mg
$85.80
1/EA
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45-B5188-50MG 50 mg
$324.00
1/EA
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assay ≥98% (HPLC)
color white to off-white
form powder
InChI 1S/C23H27N.ClH/c1-23(2,3)21-14-12-18(13-15-21)16-24(4)17-20-10-7-9-19-8-5-6-11-22(19)20;/h5-15H,16-17H2,1-4H3;1H
InChI key LJBSAUIFGPSHCN-UHFFFAOYSA-N
originator Schering Plough
Quality Level 100 
SMILES string Cl.CN(Cc1ccc(cc1)C(C)(C)C)Cc2cccc3ccccc23
solubility DMSO: ≥10 mg/mL
storage condition desiccated
storage temp. room temp
Application: Butenafine hydrochloride has been used as a standard in high-performance liquid chromatography (HPLC) method to determine butenafine hydrochloride in butenafine-loaded nanosponges.
Biochem/physiol Actions: Butenafine exhibits fungicidal and antimycotic activity. This fungal squalene epoxidase inhibitor serves as an effective fungicide against T. rubrum, T. mentagrophytes, Microsporum canis, Aspergillus fumigatus, Sporothrix schenckii, Candida parapsilosis, and C. albicans. It is considered more effective and rapid than other antifungal drugs at curing dermatophytosis and preventing recurrences. In humans, it is used topically to treat tinea conditions and superficial candidiasis. Butenafine is considered a promising antimycotic compound to treat tinea pedis due to its efficiency, safety profile, relapse rates, and cost-effectiveness.
Biochem/physiol Actions: Butenafine is an antifungal; squalene epoxidase inhibitor. It inhibits the synthesis of ergosterol needed in fungal cell membranes.
Biochem/physiol Actions: Butenafine possesses antifungal property. It is a squalene epoxidase inhibitor. Butenafine can inhibit the synthesis of ergosterol needed in fungal cell membranes.
Features and Benefits: This compound was developed by Schering Plough . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here .
General description: Butenafine hydrochloride is chemically known as N-4-tertbutylbenzyl-N-methyl-1-naphthalenemethylamine hydrochloride. Butenafine, a benzylamine derivative, is a new generation antimycotic compound. It is easily soluble in methanol, ethanol, dichloromethane, and chloroform, but not in water. The allyl radical in butenafine hydrochloride is substituted by a butylbenzyl group.
Packaging: 10, 50 mg in glass bottle
Symbol GHS07  GHS07
Signal word Warning
Hazard statements H312
Precautionary statements P280
Hazard Codes Xn
Risk Statements 21
RIDADR NONH for all modes of transport
WGK Germany nwg
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. room temp
UNSPSC 51111800

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